Aminolysis of P-trichloro-N-dichlorophosphorylmonophosphazene and the crystal structure of 1-(dichlorophosphinyl)-2-chloro-2,2-bis(diisopropylamino)phosphazene
✍ Scribed by Zeynel Kılıçc; Necla Gündüz; Mustafa Yıldız; Adem Kılıçc; Sevtap Mor; Filiz Ercan; Tuncer Hökelek; Dinçer Ülkü
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 728 KB
- Volume
- 5
- Category
- Article
- ISSN
- 1042-7163
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✦ Synopsis
The reactions of Ci3P=N-P(0)C12 (1) with primary and secondary amines have been studied. The following monophosphazenes, (RRV),P= N-P(O)(NRR),, and bis(phosphinoyl)amines, [(RRN),P(O)],NH were isolated: NRR = NHCH2Ph, NEt,, NH(CH2),CH3 groups for monophosphazenes, and NEt,, NH(CH2),CH3 for phosphinoyl arnines. The unexpected geminal phosphazene, Cl(RIW),P= N-P(O)Cl,, (RIW = N[CH(CH3)?I2}, was also obtained in moderate yield. The spectral data (ZR, ' H , C , and 3iP N M R , and M S ) are presented. The structure of 1 -(dichlorophosphinyl)-2-chloro-2,2-bis(diisopro-py1amino)phosphazene (5) was determined by X-ray crystallography. The basicities of these and related compounds in nonaqueous nitrobenzene solution were obtained bv potentiometric titration.
📜 SIMILAR VOLUMES
## Abstract The three‐dimensional structure of the title compound has been established by means of an X‐ray analysis. The product was formed by a thermal 1,3‐dipolar cycloaddition. According to the concerted [~π~4~__s__~ + ~π~2~__s__~]‐mechanism the formation of this stereoisomer should actually be